United States · FDA National Drug Code directory
Diclofenac Potassium
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 85509-2750_43069d0f-e508-d0c7-e063-6394a90a3e02
- Product NDC
- 85509-2750
- Form
- TABLET, FILM COATED
- Composition / generic term
- diclofenac potassium
- Labeler
- Phoenix RX LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241021
- Source listing expiry
- 20261231
Source-listed ingredients
- DICLOFENAC POTASSIUM — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-2750-1) · 85509-2750-1
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-2750-3) · 85509-2750-3
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-2750-6) · 85509-2750-6
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85509-2750-9) · 85509-2750-9
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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